null

SMILES CCCCCCCN(CCc1ccc(SC(C)(C)C(O)=O)cc1)C(=O)Nc1ccc(F)cc1F

InChI Key InChIKey=KYQNYMXQHLMADB-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 28799   

TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM28799(2-{[4-(2-{[(2,4-difluorophenyl)carbamoyl](heptyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibitory activity against human Peroxisome proliferator activated receptor alphaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D50MB0PubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM28799(2-{[4-(2-{[(2,4-difluorophenyl)carbamoyl](heptyl)a...)copy SMILEScopy InChI
Affinity DataEC50:  1.90E+3nMAssay Description:Cotransfection activity of compound against human Peroxisome proliferator activated receptor gamma was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D50MB0PubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM28799(2-{[4-(2-{[(2,4-difluorophenyl)carbamoyl](heptyl)a...)copy SMILEScopy InChI
Affinity DataIC50: 550nMAssay Description:Inhibitory activity of compound against the binding of human Peroxisome proliferator activated receptor gamma was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D50MB0PubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM28799(2-{[4-(2-{[(2,4-difluorophenyl)carbamoyl](heptyl)a...)copy SMILEScopy InChI
Affinity DataEC50:  340nMAssay Description:Cotransfection activity of compound against human Peroxisome proliferator activated receptor alpha was determinedMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D50MB0PubMed